Canonical Allele Identifier: CA432318289

Gene: ITPR1

Linked Data

• MyVariant Identifiers: chr3:g.4821281C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.4779597C>T , CM000665.2:g.4779597C>T	GRCh38
NC_000003.11:g.4821281C>T , CM000665.1:g.4821281C>T	GRCh37
NC_000003.10:g.4796281C>T	NCBI36
NG_016144.1:g.291250C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302640.13:c.6350C>T	ENSP00000306253.9:n.6350C>T
ENST00000354582.12:c.6315C>T	ENSP00000346595.8:p.Asp2105=
ENST00000443694.5:c.6294C>T	ENSP00000401671.2:p.Asp2098=
ENST00000354582.11:c.6315C>T	ENSP00000346595.8:p.Asp2105=
ENST00000357086.10:c.6195C>T	ENSP00000349597.4:p.Asp2065=
ENST00000443694.4:c.6294C>T	ENSP00000401671.2:p.Asp2098=
ENST00000456211.8:c.6150C>T	ENSP00000397885.2:p.Asp2050=
ENST00000544951.6:c.997-26506C>T	ENSP00000440564.1:n.997-26506C>T
ENST00000647708.1:c.2238C>T
ENST00000647717.1:n.3843C>T
ENST00000648016.1:c.2674C>T
ENST00000648038.1:c.4101C>T	ENSP00000497872.1:p.Asp1367=
ENST00000648212.1:c.3247C>T
ENST00000648266.1:c.6312C>T	ENSP00000498014.1:p.Asp2104=
ENST00000648309.1:c.6267C>T	ENSP00000497026.1:p.Asp2089=
ENST00000648390.1:c.447-66542C>T
ENST00000648431.1:c.3641C>T
ENST00000648510.1:n.173C>T
ENST00000649015.2:c.6339C>T MANE Select	ENSP00000497605.1:p.Asp2113=
ENST00000649144.1:n.1387C>T
ENST00000649694.1:n.3824C>T
ENST00000650294.1:c.6297C>T	ENSP00000498056.1:p.Asp2099=
ENST00000302640.12:c.6294C>T	ENSP00000306253.8:p.Asp2098=
ENST00000354582.10:c.6339C>T	ENSP00000346595.7:p.Asp2113=
ENST00000357086.9:c.6195C>T	ENSP00000349597.4:p.Asp2065=
ENST00000443694.3:c.6294C>T	ENSP00000401671.2:p.Asp2098=
ENST00000456211.7:c.6150C>T	ENSP00000397885.2:p.Asp2050=
ENST00000544951.5:c.997-26506C>T	ENSP00000440564.1:n.997-26506C>T
NM_001099952.2:c.6195C>T	NP_001093422.2:p.Asp2065=
NM_001168272.1:c.6294C>T	NP_001161744.1:p.Asp2098=
NM_002222.5:c.6150C>T	NP_002213.5:p.Asp2050=
XM_005265109.2:c.6270C>T	XP_005265166.1:p.Asp2090=
XM_005265110.2:c.6222C>T	XP_005265167.1:p.Asp2074=
XM_006713131.2:c.6273C>T	XP_006713194.1:p.Asp2091=
XM_011533681.1:c.6342C>T	XP_011531983.1:p.Asp2114=
XM_011533682.1:c.6342C>T	XP_011531984.1:p.Asp2114=
XM_011533683.1:c.6339C>T	XP_011531985.1:p.Asp2113=
XM_011533684.1:c.6315C>T	XP_011531986.1:p.Asp2105=
XM_011533685.1:c.6309C>T	XP_011531987.1:p.Asp2103=
XM_011533686.1:c.6306C>T	XP_011531988.1:p.Asp2102=
XM_011533687.1:c.6297C>T	XP_011531989.1:p.Asp2099=
XM_011533688.1:c.6270C>T	XP_011531990.1:p.Asp2090=
XM_011533689.1:c.6231C>T	XP_011531991.1:p.Asp2077=
XM_011533690.1:c.6342C>T	XP_011531992.1:p.Asp2114=
XM_005265109.3:c.6270C>T	XP_005265166.1:p.Asp2090=
XM_005265110.3:c.6222C>T	XP_005265167.1:p.Asp2074=
XM_006713131.3:c.6273C>T	XP_006713194.1:p.Asp2091=
XM_011533682.3:c.6342C>T	XP_011531984.1:p.Asp2114=
XM_011533683.3:c.6339C>T	XP_011531985.1:p.Asp2113=
XM_011533684.2:c.6315C>T	XP_011531986.1:p.Asp2105=
XM_011533685.2:c.6309C>T	XP_011531987.1:p.Asp2103=
XM_011533686.2:c.6306C>T	XP_011531988.1:p.Asp2102=
XM_011533687.2:c.6297C>T	XP_011531989.1:p.Asp2099=
XM_011533688.2:c.6270C>T	XP_011531990.1:p.Asp2090=
XM_011533690.2:c.6342C>T	XP_011531992.1:p.Asp2114=
XM_017006357.2:c.6339C>T	XP_016861846.1:p.Asp2113=
NM_001099952.3:c.6195C>T	NP_001093422.2:p.Asp2065=
NM_002222.6:c.6150C>T	NP_002213.5:p.Asp2050=
NM_001099952.4:c.6195C>T	NP_001093422.2:p.Asp2065=
NM_001168272.2:c.6294C>T	NP_001161744.1:p.Asp2098=
NM_001378452.1:c.6339C>T MANE Select	NP_001365381.1:p.Asp2113=
NM_002222.7:c.6150C>T	NP_002213.5:p.Asp2050=